CAS 928822-98-4

5-MeO-DALT

Description:

5-MeO-DALT, or 5-Methoxy-N,N-diallyltryptamine, is a synthetic compound belonging to the tryptamine class, which is known for its psychoactive properties. It is structurally related to other tryptamines and is characterized by the presence of a methoxy group and two allyl groups attached to the nitrogen atom. This compound is often explored for its potential effects on serotonin receptors, particularly the 5-HT2A receptor, which is implicated in mood regulation and perception. Users have reported a range of subjective effects, including altered sensory perception, enhanced emotional experiences, and introspective insights. However, the pharmacological profile of 5-MeO-DALT is not extensively studied, and its safety, efficacy, and long-term effects remain largely unknown. As with many novel psychoactive substances, there are concerns regarding purity, dosage, and potential for adverse reactions. Due to its legal status varying by jurisdiction, caution is advised for those considering its use.

Formula: C₁₇H₂₂N₂O

InChI: InChI=1S/C17H22N2O/c1-4-9-19(10-5-2)11-8-14-13-18-17-7-6-15(20-3)12-16(14)17/h4-7,12-13,18H,1-2,8-11H2,3H3

InChI key: InChIKey=HGRHWEAUHXYNNP-UHFFFAOYSA-N

SMILES: C(CN(CC=C)CC=C)C=1C=2C(NC1)=CC=C(OC)C2

Synonyms:

• 1H-Indole-3-ethanamine, 5-methoxy-N,N-di-2-propen-1-yl-
• 5-Meo-dalt
• 5-Methoxy-N,N-di-2-propen-1-yl-1H-indole-3-ethanamine
• 5-Methoxy-N,N-diallyl-1H-indole-3-ethanamine
• 5-Methoxy-N,N-diallyltryptamine
• N-allyl-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]prop-2-en-1-amine

5-MeO-DALT (5-Methoxy-N,N-diallyltryptamine)

Controlled Product

CAS: 928822-98-4

Color and Shape: Neat

Ref: 61-FOR1275.07

5-MeO-DALT (5-Methoxy-N,N-diallyltryptamine) 1.0 mg/ml in Acetonitrile

Controlled Product

CAS: 928822-98-4

Color and Shape: Single Solution

Ref: 61-AMP1275.07-11

N,N-Diallyl-5-methoxytryptamine

Controlled Product

CAS: 928822-98-4

N,N-Diallyl-5-methoxytryptamine (DMAT) is a synthetic cannabinoid that has been shown to produce effects similar to those of tetrahydrocannabinol. It has been used in clinical studies to study the effects of cannabinoids on the central nervous system. DMAT binds with high affinity to 5-HT2A receptors and low affinity to histamine H1 receptors. DMAT also binds moderately with 5-HT1A receptors, which are serotonin receptors found in the cerebral cortex and hippocampus regions of the brain. DMAT is a potent monoamine neurotransmitter reuptake inhibitor, which means it prevents the reuptake of monoamines such as dopamine, norepinephrine, and serotonin by blocking their transporters. This results in an increase in extracellular concentrations of these monoamines. DMAT is structurally similar to other drugs that have been shown to cause seizures, such as meprobamate, benzodiazepines,

Formula: C₁₇H₂₂N₂O

Purity: Min. 95%

Molecular weight: 270.37 g/mol

Ref: 3D-FD21443

N,N-Diallyl-5-methoxytryptamine

Controlled Product

CAS: 928822-98-4

Applications It is a tryptamine derivative recently used as a component in ‘bath salts’ that act directly on monoamine receptors (similar to MDMA) to produce its psychoactive effects. This compound is a standard for the forensic analysis of samples that may contain this compound.
References Kuipers, W., et al.: J. Med. Chem., 38, 1942 (1995), Green, A., et al.: Pharmacol. Rev., 55, 463 (2003), Nagai, F., et al.: Eur. J. Pharmacol., 559, 132 (2007),

Formula: C₁₇H₂₂N₂O

Color and Shape: Neat

Molecular weight: 270.369

Ref: TR-D416040